US6391874B1 - Fused heterocyclic compounds as protein tyrosine kinase inhibitors - Google Patents

Fused heterocyclic compounds as protein tyrosine kinase inhibitors Download PDF

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Publication number
US6391874B1
US6391874B1 US09/214,267 US21426798A US6391874B1 US 6391874 B1 US6391874 B1 US 6391874B1 US 21426798 A US21426798 A US 21426798A US 6391874 B1 US6391874 B1 US 6391874B1
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United States
Prior art keywords
quinazolin
alkyl
methyl
amine
benzyloxy
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Expired - Lifetime
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US09/214,267
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English (en)
Inventor
George Stuart Cockerill
Malcolm Clive Carter
Stephen Barry Guntrip
Kathryn Jane Smith
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Novartis AG
GlaxoSmithKline Research and Development Ltd
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SmithKline Beecham Corp
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Priority claimed from GBGB9614755.8A external-priority patent/GB9614755D0/en
Priority claimed from GBGB9625458.6A external-priority patent/GB9625458D0/en
Application filed by SmithKline Beecham Corp filed Critical SmithKline Beecham Corp
Assigned to GLAXO RESEARCH AND DEVELOPMENT LIMITED reassignment GLAXO RESEARCH AND DEVELOPMENT LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CARTER, MALCOLM C., COCKERILL, GEORGE S., GUNTRIP, STEPHEN B., SMITH, KATHRYN J.
Assigned to GLAXO WELLCOME INC., GLAXO RESEARCH AND DEVELOPMENT LIMITED reassignment GLAXO WELLCOME INC. CORRECTIVE ASSIGNMENT TO CORRECT ASSIGNEE'S NAME, Assignors: CARTER, MALCOLM C., COCKERILL, GEORGE S., GUNTRIP, STEPHEN B., SMITH, KATHRYN J.
Priority to US10/062,647 priority Critical patent/US6828320B2/en
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Publication of US6391874B1 publication Critical patent/US6391874B1/en
Assigned to SMITHKLINE BEECHAM (CORK) LIMITED reassignment SMITHKLINE BEECHAM (CORK) LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SMITHKLINE BEECHAM CORPORATION
Assigned to SMITHKLINE BEECHAM CORPORATION reassignment SMITHKLINE BEECHAM CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SMITHKLINE BEECHAM (CORK) LIMITED
Assigned to GLAXOSMITHKLINE LLC reassignment GLAXOSMITHKLINE LLC CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: SMITHKLINE BEECHAM CORPORATION
Assigned to LEO OSPREY LIMITED reassignment LEO OSPREY LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GLAXOSMITHKLINE LLC
Assigned to NOVARTIS AG reassignment NOVARTIS AG ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LEO OSPREY LIMITED
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Definitions

  • R 1 and R 2 together form specified optionally substituted groups containing at least one heteroatom so as to form a 5 or 6-membered ring, in which there is a N atom at the 6 position of the quinazoline ring;
  • R 3 includes independently hydrogen, hydroxy, halogeno, (1-4C)alkyl, (1-4C) alkoxy di-[(1-4C)alkyl]amino, or (2-4C)alkanoylamino.
  • R 3 represents a group selected from M 1 —M 2 —M 3 —M 4 , M 1 —M 5 or M 1 —M 2 —M 3′ —M 6 wherein
  • M 1 represents CH 2 , CO, CH 2 CH 2 or CH 2 CO, more preferably CH 2 .
  • R 16 represents OH, NH 2 , N(C 1-4 alkyl) 2 or OC 1-4 alkyl; more preferably R 16 represents NH 2 or N(CH 3 ) 2 .
  • M 1 —M 5 represents a piperidonyl-methyl, pyrrolidinonyl-methyl or dioxoimidazolidinyl-methyl group.
  • Such processes are especially suitable for the preparation of compounds of formula (I) wherein p is 0 and R 1 carries a substituent selected from M 1 —M 2 —M 3 —M 4 , M 1 —M 5 or M 1 —M 2 —M 3′ —M 6 as defined above in which M 2 represents CR 12 R 13 .
  • 6-(1,2,3,4-Tetrazol-5-yl)-quinazolin-4-one (3.31 g) was treated with acetic anhydride (115 ml) at reflux under N 2 for 1 hour. The anhydride was removed in vacuo, the residue absorbed onto silica and purified by chromatography to give the title compound as a white solid (3.47 g). The analytical data was consistent with that given earlier.

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
US09/214,267 1996-07-13 1997-07-11 Fused heterocyclic compounds as protein tyrosine kinase inhibitors Expired - Lifetime US6391874B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US10/062,647 US6828320B2 (en) 1996-07-13 2002-01-31 Heterocyclic compounds

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB9614755 1996-07-13
GBGB9614755.8A GB9614755D0 (en) 1996-07-13 1996-07-13 Heterocyclic compounds
GBGB9625458.6A GB9625458D0 (en) 1996-12-07 1996-12-07 Heterocyclic compounds
GB9625458 1996-12-07
PCT/EP1997/003672 WO1998002434A1 (en) 1996-07-13 1997-07-11 Fused heterocyclic compounds as protein tyrosine kinase inhibitors

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1997/003672 A-371-Of-International WO1998002434A1 (en) 1996-07-13 1997-07-11 Fused heterocyclic compounds as protein tyrosine kinase inhibitors

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US10/062,647 Continuation US6828320B2 (en) 1996-07-13 2002-01-31 Heterocyclic compounds

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US09/214,267 Expired - Lifetime US6391874B1 (en) 1996-07-13 1997-07-11 Fused heterocyclic compounds as protein tyrosine kinase inhibitors
US10/062,647 Expired - Lifetime US6828320B2 (en) 1996-07-13 2002-01-31 Heterocyclic compounds

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US (2) US6391874B1 (cg-RX-API-DMAC7.html)
EP (1) EP0912559B1 (cg-RX-API-DMAC7.html)
JP (1) JP4386967B2 (cg-RX-API-DMAC7.html)
AR (1) AR007857A1 (cg-RX-API-DMAC7.html)
AT (1) ATE227283T1 (cg-RX-API-DMAC7.html)
AU (1) AU3766897A (cg-RX-API-DMAC7.html)
CY (1) CY2451B1 (cg-RX-API-DMAC7.html)
DE (1) DE69716916T2 (cg-RX-API-DMAC7.html)
DK (1) DK0912559T3 (cg-RX-API-DMAC7.html)
ES (1) ES2186908T3 (cg-RX-API-DMAC7.html)
ID (1) ID19609A (cg-RX-API-DMAC7.html)
PT (1) PT912559E (cg-RX-API-DMAC7.html)
WO (1) WO1998002434A1 (cg-RX-API-DMAC7.html)

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